Detalhe da pesquisa
1.
Human prefrontal cortex gene regulatory dynamics from gestation to adulthood at single-cell resolution.
Cell
; 185(23): 4428-4447.e28, 2022 11 10.
Artigo
Inglês
| MEDLINE | ID: mdl-36318921
2.
Deep sequencing of short capped RNAs reveals novel families of noncoding RNAs.
Genome Res
; 2022 Aug 12.
Artigo
Inglês
| MEDLINE | ID: mdl-35961773
3.
An atlas of combinatorial transcriptional regulation in mouse and man.
Cell
; 140(5): 744-52, 2010 Mar 05.
Artigo
Inglês
| MEDLINE | ID: mdl-20211142
4.
Stromal cell diversity associated with immune evasion in human triple-negative breast cancer.
EMBO J
; 39(19): e104063, 2020 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32790115
5.
Comparative transcriptomics of primary cells in vertebrates.
Genome Res
; 30(7): 951-961, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32718981
6.
Correction: MaxHiC: A robust background correction model to identify biologically relevant chromatin interactions in Hi-C and capture Hi-C experiments.
PLoS Comput Biol
; 18(9): e1010515, 2022 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-36083878
7.
MaxHiC: A robust background correction model to identify biologically relevant chromatin interactions in Hi-C and capture Hi-C experiments.
PLoS Comput Biol
; 18(6): e1010241, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35749574
8.
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis.
Brain
; 145(11): 3985-3998, 2022 11 21.
Artigo
Inglês
| MEDLINE | ID: mdl-34957489
9.
An atlas of human long non-coding RNAs with accurate 5' ends.
Nature
; 543(7644): 199-204, 2017 03 09.
Artigo
Inglês
| MEDLINE | ID: mdl-28241135
10.
Comprehensive Characterization of Transcriptional Activity during Influenza A Virus Infection Reveals Biases in Cap-Snatching of Host RNA Sequences.
J Virol
; 94(10)2020 05 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32161175
11.
Human genetics and genomics meetings going virtual: practical lessons learned from two international meetings in early 2020.
Hum Genomics
; 14(1): 27, 2020 07 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32641116
12.
Bi-allelic mutations in MYL1 cause a severe congenital myopathy.
Hum Mol Genet
; 27(24): 4263-4272, 2018 12 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30215711
13.
scMatch: a single-cell gene expression profile annotation tool using reference datasets.
Bioinformatics
; 35(22): 4688-4695, 2019 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31028376
14.
Systematic analysis of transcription start sites in avian development.
PLoS Biol
; 15(9): e2002887, 2017 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-28873399
15.
A promoter-level mammalian expression atlas.
Nature
; 507(7493): 462-70, 2014 Mar 27.
Artigo
Inglês
| MEDLINE | ID: mdl-24670764
16.
An atlas of active enhancers across human cell types and tissues.
Nature
; 507(7493): 455-461, 2014 Mar 27.
Artigo
Inglês
| MEDLINE | ID: mdl-24670763
17.
Integration of genetics and miRNA-target gene network identified disease biology implicated in tissue specificity.
Nucleic Acids Res
; 46(22): 11898-11909, 2018 12 14.
Artigo
Inglês
| MEDLINE | ID: mdl-30407537
18.
Analysis of the human monocyte-derived macrophage transcriptome and response to lipopolysaccharide provides new insights into genetic aetiology of inflammatory bowel disease.
PLoS Genet
; 13(3): e1006641, 2017 03.
Artigo
Inglês
| MEDLINE | ID: mdl-28263993
19.
New era in genetics of early-onset muscle disease: Breakthroughs and challenges.
Semin Cell Dev Biol
; 64: 160-170, 2017 04.
Artigo
Inglês
| MEDLINE | ID: mdl-27519468
20.
Identification of novel cerebellar developmental transcriptional regulators with motif activity analysis.
BMC Genomics
; 20(1): 718, 2019 Sep 18.
Artigo
Inglês
| MEDLINE | ID: mdl-31533632